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dc.contributor.authorReddy, P S N-
dc.contributor.authorReddy, P Pratap-
dc.contributor.authorVasantha, T-
dc.date.accessioned2013-10-04T11:10:29Z-
dc.date.available2013-10-04T11:10:29Z-
dc.date.issued2003-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21521-
dc.description393-396en_US
dc.description.abstract2-Chloromethyl-3-methylquinazolin-4(3H)-one 1 is converted to the azide 4 which easily undergoes cyclisation to give 2- quinazolinonyl imidazolidinones 5. The azides, however, yield 2,3-dimethylquinazolin-4(3H)-one 6 and/or 2-aryl-aminomethyl-3-methylquinazolin-4(3H)-one 2 under thermal, microwave and in acidic medium.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.42B(02) [February 2003]en_US
dc.titleSynthesis of 2-quinazolinonyl imidazolidinonesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(02) [February 2003]

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